United Foods Public Co., Ltd.
FDA import alert and refusal historyBangkhuntien, ThailandFEI 1000177017
Recorded by FDA as UNITED FOODS PUBLIC CO., LTD.
As of October 26, 2026, United Foods Public Co., Ltd. (Bangkhuntien, Thailand) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for yoyo gummy assorted; yoyo gummy grape plus; yoyo gummy tropical flavor; motta jelly squeezable jelly, published by FDA on September 18, 2009, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 45-02 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for United Foods Public Co., Ltd.
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 45-02red listYOYO Gummy Assorted; YOYO Gummy Grape Plus; YOYO Gummy Tropical Flavor; motta jelly squeezable jellySource
Questions about United Foods Public Co., Ltd.
- Is United Foods Public Co., Ltd. on an FDA import alert?
- Yes. As of October 26, 2026, United Foods Public Co., Ltd. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for yoyo gummy assorted; yoyo gummy grape plus; yoyo gummy tropical flavor; motta jelly squeezable jelly; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from United Foods Public Co., Ltd.?
- No FDA import refusals for United Foods Public Co., Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is United Foods Public Co., Ltd.'s FEI number?
- United Foods Public Co., Ltd.'s FDA Establishment Identifier (FEI) is 1000177017.
- Can shipments from United Foods Public Co., Ltd. still enter the U.S.?
- Shipments of yoyo gummy assorted; yoyo gummy grape plus; yoyo gummy tropical flavor; motta jelly squeezable jelly from United Foods Public Co., Ltd. can be detained without physical examination under Import Alert 45-02; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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